Canonical Allele Identifier: CA501023717

Gene: MPO

Linked Data

• MyVariant Identifiers: chr17:g.56351025G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58273664G>T , CM000679.2:g.58273664G>T	GRCh38
NC_000017.10:g.56351025G>T , CM000679.1:g.56351025G>T	GRCh37
NC_000017.9:g.53706024G>T	NCBI36
NG_009629.1:g.12272C>A , LRG_84:g.12272C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000578493.2:n.704C>A
ENST00000699291.1:c.496C>A	ENSP00000514272.1:p.His166Asn
ENST00000699292.1:n.411C>A
ENST00000225275.4:c.1371C>A MANE Select	ENSP00000225275.3:p.Ile457=
ENST00000225275.3:c.1371C>A	ENSP00000225275.3:p.Ile457=
NM_000250.1:c.1371C>A , LRG_84t1:c.1371C>A	NP_000241.1:p.Ile457=
XM_011524821.1:c.1557C>A	XP_011523123.1:p.Ile519=
XM_011524822.1:c.1086C>A	XP_011523124.1:p.Ile362=
XM_011524823.1:c.1396C>A	XP_011523125.1:p.His466Asn
NM_000250.2:c.1371C>A MANE Select	NP_000241.1:p.Ile457=